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3-Nitrophenacylamine Hydrochloride, a chemical compound with the chemical formula C8H9ClN2O2, is often utilized in scientific research and experimental works. It typically appears as a yellowish or light brown powder and is known for its unique physical and chemical properties that make it valuable in organic reactions. Due to its potential risks, such as skin irritation or serious eye irritation, it should be handled and stored carefully following Material Safety Data Sheet (MSDS) guidelines.

36765-84-1

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36765-84-1 Usage

Uses

Used in Scientific Research:
3-Nitrophenacylamine Hydrochloride is used as a reagent in various scientific research applications for its distinctive properties that facilitate specific organic reactions.
Used in Laboratory Experiments:
In laboratory settings, 3-Nitrophenacylamine Hydrochloride is used as a compound in experimental procedures, where its chemical characteristics contribute to the understanding and development of new chemical processes and products.
While there is no absolute evidence specifying its wide use in industries such as pharmaceuticals, agriculture, or cosmetics, the compound's potential applications in these fields could be explored further, given its unique properties and reactivity in organic reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 36765-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,6 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36765-84:
(7*3)+(6*6)+(5*7)+(4*6)+(3*5)+(2*8)+(1*4)=151
151 % 10 = 1
So 36765-84-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O3/c9-5-8(11)6-2-1-3-7(4-6)10(12)13/h1-4H,5,9H2/p+1

36765-84-1 Well-known Company Product Price

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  • Alfa Aesar

  • (A12205)  2-Amino-3'-nitroacetophenone hydrochloride, 98%   

  • 36765-84-1

  • 1g

  • 748.0CNY

  • Detail
  • Alfa Aesar

  • (A12205)  2-Amino-3'-nitroacetophenone hydrochloride, 98%   

  • 36765-84-1

  • 5g

  • 1880.0CNY

  • Detail

36765-84-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1-(3-nitrophenyl)ethanone,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-NITROPHENACYLAMINE HYDROCHLORIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:36765-84-1 SDS

36765-84-1Relevant academic research and scientific papers

Design, synthesis and biological evaluation of new aryl thiosemicarbazone as antichagasic candidates

Blau, Lorena,Menegon, Renato Farina,Trossini, Gustavo H. G.,Molino, Jo?o Vitor Dutra,Vital, Drielli Gomes,Cicarelli, Regina Maria Barretto,Passerini, Gabriela Duó,Bosquesi, Priscila Longhin,Chin, Chung Man

, p. 142 - 151 (2013/10/01)

The present work reports on the synthesis, biological assaying and docking studies of a series of 12 aryl thiosemicarbazones, which were planned to act over two main enzymes, cruzain and trypanothione reductase. These enzymes are used as targets of trypanocidal activity in Chagas disease control with a minimal mutagenic profile. Three p-nitroaromatic thiosemicarbazones showed high activity against Trypanosoma cruzi in in vitro assays (IC50 57 μM), and no mutagenic profile was observed in micronucleous tests. Although the in vitro inhibition test showed that 10-μM doses of eight compounds inhibited cruzain activity, no correlation was found between cruzain inhibition and trypanocidal activity.

Thiadizines

-

, (2008/06/13)

Novel heterocyclic compounds of the formula: STR1 wherein either X is --CR1 R2 -- and Y is oxygen, sulphur or --NR3, wherein R1, R2 and R3, which may be the same or different, each is hydrogen or alkyl of up to 4 carbon atoms; or X is oxygen, sulphur or --NH-- and Y is --CH2 --; wherein R4 and R5, which may be the same or different, each is hydrogen, cyano, nitro, amino or hydroxy, or alkylthio of up to 4 carbon atoms, or has various other meanings defined in claim 1, provided that R4 and R5 are not both hydrogen; or wherein R4 and R5 are joined together such that with the benzene ring A they form a benzheterocyclic ring as defined in claim 1; and therein the benzene ring A may optionally bear one or more further substituents; or a salt thereof where appropriate. These compounds possess cardiotonic properties, and some of them possess peripheral vasodilator properties, and they are useful for the treatment of acute or chronic heart failure. Representative of the compounds is N,N-dimethyl-p-(5,6-dihydro-5-oxo-4H-1,3,4-thiadiazin-2-yl)benzamide. Also disclosed are processes for the manufacture of the compounds and pharmaceutical compositions containing them.

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